Nasal cannula

ABSTRACT

A nasal cannula arrangement for use as part of systems for delivery respiratory gases to a patient is disclosed. The nasal cannula arrangement includes a manifold part adapted to receive gases from a delivery conduit. The manifold includes one but preferably a pair of prongs extending upward and curving towards the rear of the manifold. The prongs are inserted into the nostrils of the patient and deliver gases to a patient. The prongs have a cut out on the rear side of the prongs. The cut out forms a gases outlet in the prongs and are shaped such that the area of the cut out area is greater than the cross sectional area of the prongs at the entry point to the prongs.

INCORPORATION BY REFERENCE TO ANY PRIORITY APPLICATIONS

Any and all applications for which a foreign or domestic priority claimis identified in the Application Data Sheet as filed with the presentapplication are hereby incorporated by reference under 37 CFR 1.57.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to nasal cannula arrangements forsupplying gases to a user via the nasal passages. The present inventionalso relates to a system which provides gases to a patient or user viathe nasal passages. The present invention also relates to a method ofsupplying gases to a user via the nasal passages.

2. Description of the Related Art

The prior art includes a wide variety of interfaces for supplying gasesto a patient. These interfaces are frequently used for delivering astream of gases to a person being treated for a sleep disorder, or fordelivery of supplementary gases to a user who is breathing unaided, butwho requires these supplementary gases. These users typically wear theinterface in a hospital Intensive Care Unit (ICU), other hospital wardsor a home sleeping environment. Comfort even under conditions of patientmovement is a major consideration.

The following are examples of interface types known in the prior art.

The prior art includes a nasal cannula interface. A typical nasalcannula interface includes a plenum portion and entry tubing or amanifold section (symmetric or single sided) that rests against theupper lip of the user in use, and a pair of open-ended prongs, whichprotrude from the entry tubing and extend into the nostrils of the userin use to supply the patient with gases. Generally, but not always,these prongs are sized and shaped so that they do not seal against thenostrils of a patient. Nasal cannulae are used because these areadvantageous in certain situations. For example, in circumstances wherea patient is breathing normally, but requires supplementary gases suchas supplementary oxygen. The existing market for nasal cannula is wellserviced by devices suitable for delivery of gases in the 0 to 5 litresper minute range. These devices are typically supported by a doubleentry lumen of small diameter (2-3 mm range) that supplies both sides ofthe nasal cannula and provides even or equal airflow to each nasalprong. These devices work well for the delivery of dry gas flows ofbetween 0 to 5 litres per minute, when the patient is self-breathing,and it is not necessary for the cannula prongs to seal against the naresof a user. A user will entrain the supplementary gases provided from thecannula along with atmospheric air as they inhale normally.

An example of a nasal cannula interface that seals against the nostrilsis the Nasal-Aire interface made by Innomed, where gases are provided tothe interface and the prongs by conduits or hoses that extend from theusers nose across their cheeks, over their cars and around the back oftheir head.

WO 2008/060295 describes a non-sealing cannula that includes nasalprongs. There are many configurations described. The nasal prongs areadapted to deliver air to a patient's nasal passage and the differentembodiments of prongs described include various external features, andmay include passages that pass through the wall of the prongs to allowsensors or similar to measure the properties of gases in the prongs.

The prior art also includes several other types of interface, which areincluded here for general context, but which are not directly relevant.These are outlined briefly below.

A nasal mask, which includes a perimeter seal that seals across, downeach cheek alongside the nose and along the surface of the upper lip.The entire enclosed space is pressurised and the recipient may inhalethe pressurised gas from the enclosed space. An example is the Flexifit405 nasal mask sold by Fisher & Paykel Healthcare.

A full face mask, which includes a perimeter seal that extends acrossthe bridge of the nose downward along each cheek beside the nose to thejaw and along the jaw below the lower lip. The perimeter therebyencloses both the nose and mouth. The entire space within the mask frameis pressurised. The recipient may breathe the pressurised gas from thespace through either the nose or mouth. An example is the Hexifit 431interface sold by Fisher & Paykel Healthcare.

An oral interface including an oral appliance that fits within theuser's mouth. An example is the Fisher & Paykel Healthcare Oracleinterface.

Nasal pillows, which are intended to seal around the perimeter of auser's wires in use, and deliver a stream of pressurised gases to thenasal cavity of a user. A number of different types of nasal pillow aredescribed and shown in WO 2008/014543.

In this specification where reference has been made to patentspecifications, other external documents, or other sources ofinformation, this is generally for the purpose of providing a contextfor discussing the features of the invention. Unless specifically statedotherwise, reference to such external documents is not to be construedas an admission that such documents, or such sources of information, inany jurisdiction, are prior art, or form part of the common generalknowledge in the art.

It is an object of the present invention to provide a nasal interfacewhich goes some way to overcoming the disadvantages of the prior art orwhich will at least provide the industry and public with a usefulalternative.

SUMMARY OF THE INVENTION

The term “comprising” as used in this specification means “consisting atleast in part of”. When interpreting each statement in thisspecification that includes the term “comprising”, features other thanthat or those prefaced by the term may also be present. Related termssuch as “comprise” and “comprises” are to be interpreted in the samemanner.

In a first aspect the invention can be said to broadly consist in anasal cannula arrangement for use as part of a system for deliveringrespiratory gas to a patient, said system of the type that has a gasessource adapted to provide a stream of gases to the nares of a user inuse, and a delivery conduit that in use connects between said gasessource and said nasal cannula arrangement, said nasal cannulaarrangement comprising: a gases inlet manifold part adapted in fluidconnection with said delivery conduit in use, so that said stream ofgases is delivered into said manifold part, at least one and preferablya pair of nasal prongs in fluid connection with said gases inletmanifold part and adapted to be inserted into the nares of said user,said stream of gases passing through said gases inlet manifold part andthrough said prongs, said nasal prong or prongs having a gases exitcut-out on the rear side of said prong or prongs, said gases exitcut-out having a cross-sectional area greater than the cross-sectionalarea of said prong at or close to the point of entry of said gases tosaid prong or prongs.

In a second aspect the invention may broadly be said to consist in asystem for delivering respiratory gases to a patient, said systemcomprising a gas source unit, adapted to provide a stream of gases, apatient interface, a delivery conduit which may or may not also have asecondary gases inlet conduit, adapted to receive respiratory gases fromsaid gas source and carry respiratory gases from said gas source to saidpatient interface, and a nasal cannula arrangement comprising: a gasesinlet manifold part adapted to form a fluid connection with saiddelivery conduit in use, so that said stream of gases is delivered intosaid manifold part, at least one and preferably a pair of nasal prongsin fluid connection with said gases inlet manifold part and adapted tobe inserted into the nares of said user, said stream of gases passingthrough said gases inlet manifold part and through said prongs, saidnasal prong or prongs having a gases exit cut-out on the rear side ofsaid prong or prongs, said gases exit cut-out having a cross-sectionalarea greater than the cross-sectional area of said prong at or close tothe point of entry of said gases to said prong or prongs.

In a third aspect the invention may broadly be said to consist in anasal cannula arrangement for use as part of a system for deliveringrespiratory gas to a patient, said system of the type that comprises agases source adapted to provide a stream of gases, and a deliveryconduit that in use connects between said gases source and said nasalcannula arrangement, said nasal cannula arrangement comprising: amanifold section connected to one end of said delivery conduit so thatin use said stream of gases is delivered from said delivery conduit tosaid manifold section, a pair of carrier tubes connected to saidmanifold section, so that said stream of gases is delivered from saidmanifold section to said carrier tubes, a pair of nasal prongs connectedone each to each of said carrier tubes, said nasal prongs adapted to beinserted into a patient's nares, said stream of gases passing throughthe carrier tubes, through the nasal prongs and into the patient'snares, each of said nasal prongs having a gases exit cut-out on the rearside of said prong or prongs, said gases exit cut-out having across-sectional area greater than the cross-sectional area of said prongat or close to the point of entry of said gases to said prong or prongs.

In a fourth aspect the invention may broadly be said to consist in anasal cannula arrangement for use as part of a system for deliveringrespiratory gas to a patient, said system of the type that comprises agases source adapted to provide a stream of gases to the nares of a userin use, and a delivery conduit that in use connects between said gasessource and said nasal cannula arrangement, said nasal cannulaarrangement comprising: a gases inlet manifold part adapted to form afluid connection with said delivery conduit in use, so that said streamof gases is delivered into said manifold part, at least one andpreferably a pair of nasal prongs in fluid connection with said gasesinlet manifold part and adapted to be inserted into the nares of saidpatient in use, said stream of gases passing in use through said gasesinlet manifold part and said nasal prongs, and into said users nares,each or both of said nasal prong or prongs having a gases exit cut-outon the rear side of said prong or prongs, said gases exit cut-out havinga cross-sectional area greater than the cross-sectional area of saidprong at or close to the point of entry of said gases to said prong orprongs, and wherein said at least one or both of said nasal prong orprongs is shaped so that the velocity of gases exiting said prong isreduced in comparison to the velocity of gases at or close to the pointof entry to said prong.

In a fifth aspect the invention may broadly be said to consist in anasal cannula arrangement for use as part of a system for deliveringrespiratory gas to a patient, said system of the type that comprises agases source adapted to provide a stream of gases to the nares of a userin use, and a delivery conduit that in use connects between said gasessource and said nasal cannula arrangement, said nasal cannulaarrangement comprising: a gases inlet manifold part adapted to form afluid connection with said delivery conduit in use, so that said streamof gases is delivered into said manifold part, at least one andpreferably a pair of nasal prongs in fluid connection with said gasesinlet manifold part and adapted to be inserted into the nares of saidpatient in use, said stream of gases passing in use through said gasesinlet manifold part and said nasal prongs, and into said users nares,each or both of said nasal prong or prongs having a gases exit cut-outon the rear side of said prong or prongs, said gases exit cut-out havinga cross-sectional area greater than the cross-sectional area of saidprong at or close to the point of entry of said gases to said prong orprongs, and wherein said at least one or both of said nasal prong orprongs is shaped, or sized, or shaped and sized, so that said stream ofgases is generally directed towards the back of the patient's nasalpassage.

In a sixth aspect the invention may broadly be said to consist in amethod of providing a stream of gases to a user for therapeuticpurposes, comprising the steps of: 1. fitting said user with a nasalcannula arrangement, 2. connecting said nasal cannula arrangement to apatient interface which in use holds said nasal cannula arrangement inposition on said user, 3. connecting either said patient interface oralternatively connecting said nasal cannula arrangement directly to agases delivery system of the type that comprises a gases source adaptedto provide a stream of gases, and a delivery conduit that in useconnects between said gases source and said nasal cannula arrangement,and using said system to deliver a stream of gases to said nasal cannulaarrangement, said nasal cannula arrangement comprising: a gases inletmanifold part adapted to form a fluid connection with delivery conduitin use, so that said stream of gases is delivered into said manifoldpart, at least one and preferably a pair of nasal prongs in fluidconnection with said gases inlet manifold part and adapted to beinserted into the nares of said user, said stream of gases passingthrough said gases inlet manifold part and through said prongs, saidnasal prong or prongs having a gases exit cut-out on the rear side ofsaid prong or prongs, said gases exit cut-out having a cross-sectionalarea greater than the cross-sectional area of said prong at or close tothe point of entry of said gases to said prong or prongs.

In a seventh aspect the invention may broadly be said to consist in anasal cannula arrangement for use as part of a system for deliveringrespiratory gas to a patient, said system of the type that comprises agases source adapted to provide a stream of gases to the mires of a userin use, and a delivery conduit that in use connects between said gasessource and said nasal cannula arrangement, said nasal cannulaarrangement comprising: a gases inlet manifold part adapted to form afluid connection with said delivery conduit in use, so that said streamof gases is delivered into said manifold part, at least one andpreferably a pair of nasal prongs in fluid connection with said gasesinlet manifold part and adapted to be inserted into the nares of saidpatient in use, said stream of gases passing in use through said gasesinlet manifold part and said nasal prongs, and into said users nares,each or both of said nasal prong or prongs having a gases exit cut-outon the rear side of said prong or prongs, said gases exit cut-out havinga cross-sectional area greater than the cross-sectional area of saidprong at or close to the point of entry of said gases to said prong orprongs, and wherein said at least one or both of said nasal prong orprongs is shaped so that the velocity of gases exiting said prong isreduced in comparison to the velocity of gases at or close to the pointof entry to said prong, and so that said stream of gases is generallydirected towards the back of the patient's nasal passage.

In an eighth aspect the invention may broadly be said to consist in anasal cannula arrangement for use as part of a system for deliveringrespiratory gas to a patient, said system of the type that comprises agases source adapted to provide a stream of gases to the nares of a userin use, and a delivery conduit that in use connects between said gasessource and said nasal cannula arrangement, said nasal cannulaarrangement comprising: a gases inlet manifold part adapted to form afluid connection with said delivery conduit in use, so that said streamof gases is delivered into said manifold part, at least one andpreferably a pair of nasal prongs in fluid connection with said gasesinlet manifold part and adapted to be inserted into the nares of saiduser, said stream of gases passing through said gases inlet manifoldpart and through said prongs, each prong having an upstream transitionsection and a downstream transition section, connecting the horizontallyoriented manifold with upwardly oriented prong, wherein said upstreamtransition section having a shallow curve relative to the downstreamtransition section.

Preferably said cannula arrangement includes a face mount part thatrests against a user's face in use, said face mount part including apair of side straps extending from said face mount part.

Preferably said face mount part stabilises said cannula arrangement onsaid user's face in use by resting against the user's face.

Preferably said cut-out extends between halfway and two-thirds of theway along said nasal prong, said cut-out measured from the top tip ofsaid nasal prong.

Alternatively said cut-out extends less than halfway along the nasalprong, said cut-out measured from the top tip of said nasal prong.

Alternatively said cut-out extends the entire length of the nasalprongs.

Preferably said cut-out has a height of between 3 mm and 15 mm.

Preferably said gases exit cut-out is oval in shape, when viewed fromthe rear of said nasal cannula arrangement.

Alternatively said gases exit cut-out is rectangular in shape, whenviewed from the rear of said nasal cannula arrangement.

Alternatively said cut-out is triangular in shape, when viewed from therear of said nasal cannula arrangement.

Preferably said nasal prongs are angled between 5 and 20 degrees inwardrelative to a vertical planar line which bisects said face mount part.

Preferably said nasal prongs are angled 15 degrees inward relative to avertical planar line which bisects said face mount part.

Preferably the edges of said gases exit cut-out are shaped cut-outconform to a surface that substantially has a reverse S-shape, saidS-shape aligned substantially vertically.

Preferably the lower edge of said surfacccuts across the rear of saidprongs to create said cut-out, said surface being a reverse S-shape toobtain the ideal cut-out shape.

Preferably said at least one nasal prong includes a reinforcing feature.

Preferably said reinforcing feature is located on the front face of saidnasal prong and is adapted to help prevent the nasal prong fromcollapsing under compressive or tensile forces.

Preferably said reinforcing feature is formed as a substantiallyvertical ridge or spine running at least part of the way along the frontface of said nasal prong.

Alternatively said at least one nasal prong includes a reinforcingfeature on the inner surface of the front wall of said nasal prong, toaid in preventing the nasal prong from collapsing under tensile orcompressive forces.

Preferably said at least one nasal prong includes at least one andpreferably a plurality of ribs running across the front face of thenasal prong.

Preferably said at least one rib or ribs run across the outer surface ofthe front of said nasal prong.

Preferably the front part of the wall of said nasal prong wall isthicker than the back part of the wall of the nasal prong wall.

Preferably said feature or ribs or both are formed integrally with thenasal prong.

Alternatively said feature or ribs or both are separately attached tosaid prong after said prong is formed.

Preferably said nasal cannula arrangement further includes side strapsadapted to allow a headgear securement assembly to he connected to saidnasal cannula arrangement, so that said nasal cannula arrangement can besecured to said patients head in use.

Preferably said face mount portion, said at least one nasal prong, andat least part of said side straps are formed of a flexible polymermaterial, for example a thermoplastic elastomer or silicone.

Preferably said feature or ribs or both are made of the same material assaid nasal prong.

Preferably said at least one or both of said nasal prong or prongs isshaped, or sized, or shaped and sized, so that said stream of gases isgenerally directed towards the back of the patient's nasal passage.

Preferably at least one or both nasal prong or prongs is shaped so thatthe velocity of gases exiting said prong is reduced in comparison to thevelocity of gases at or close to the point of entry to said prong.

Preferably at least one or both of said nasal prong or prongs curveupwards and backwards towards a user in use, and said cut-out has anelongate shape along the rear and the top of said prong or prongs, sothat said stream of gases is generally directed to the back of thepatient's nasal passage and jetting effects are reduced.

Preferably said nasal prongs are shaped and sized so that they do notform a substantially air tight seal with the users nares in use.

Preferably the nasal prongs are suitable for delivering high flowmedical gases to a patient; such that a substantial part of thepatient's inhaled breath composes respiratory gases from the nasalprongs and a minimal percentage of ambient air.

Preferably the cannula arrangement includes a face mount part attachedto said manifold, said face mount part resting against top lip of saidpatient, to stabilise said cannula on said patient's face.

Preferably said manifold section is a Y or T piece connector.

Preferably said nasal prongs are integral to the carrier conduit.

Preferably each said transition section transitioning from a horizontalto an upright orientation within an area, said area of transitiondefined by vertical rise and a horizontal run, said rise for saidupstream and downstream transition sections being substantially equal toeach other, said upstream transition section having a horizontal runbeing between one and two and a half times the horizontal run of saiddownstream transition section.

Preferably said rise and run is defined from a starting point being atangent point of said manifold and a finishing point being the narrowestpoint of said prong.

Preferably said upstream transition section having a horizontal run oneand half times the horizontal run of said downstream transition section.

Preferably said manifold flow chamber including an upwardly angled wallpositioned opposite the upstream prong, said wall deflecting said gasesstream by at least 20 degrees upward substantially toward the base ofsaid prong.

Preferably said downstream transition section angled upward at a steeperangle than said upstream transition section.

Preferably said downstream transition section having an upward anglebetween 1.1 to 2.5 larger than the upward angle of said upstreamtransition section.

More preferably said downstream transition section having an upwardangle 1.5 times greater than the upward angle of said upstreamtransition section.

This invention may also be said broadly to consist in the parts,elements and features referred to or indicated in the specification ofthe application, individually or collectively, and any or allcombinations of any two or more of said parts, elements or features, andwhere specific integers are mentioned herein which have knownequivalents in the art to which this invention relates, such knownequivalents are deemed to be incorporated herein as if individually setforth.

The term “comprising” as used in the specification means “consisting atin part of”. When interpreting each statement in this specification thatincludes the term “comprising”, features other than that or thoseprefaced by the term may also be present. Related terms such as“comprise” and “comprises” are to be interpreted in the same manner.

BRIEF DESCRIPTION OF THE DRAWINGS

While the invention is susceptible to embodiment in different forms,specific embodiments are shown in the drawings, and described in detail.The present disclosure is to be considered an exemplification of theprinciples of the invention, and is not intended to limit the inventionto that as illustrated and described herein.

FIG. 1 shows a respiratory humidification system that includes a blowerunit, a humidifier unit gaseously connected to the gases source unit, agases supply conduit connected to an outlet of the humidifier unit, anda patient interface, the patient interface connecting between the gasessupply conduit and a user so that gases can be provided to the user fromthe respiratory humidification system via the patient interface, thepatient interface including a nasal cannula.

FIG. 2 shows a perspective view of the preferred embodiment of thepatient interface in use on a user, the preferred form of patientinterface including a secondary supply conduit which connects betweenthe outlet end of the gases supply conduit and the nasal cannula, and aneck tie or lanyard which in use loops around the neck of a patient andconnects to the supply conduit at or close to the outlet end to supportthe weight of the supply conduit in use, the patient interface alsoincluding a head strap for securing the patient interface to a patient'shead in use.

FIG. 3 shows a front and a side view of an alternative embodiment of thepatient interface in use, this alternative form having a pair of earstraps that loop around the ears of a user in use to hold the patientinterface in place on the face of a user in use.

FIG. 4 shows a perspective view from the front and to one side of themost preferred form of nasal cannula, the nasal cannula of the preferredform having a face mount part and a manifold part, the manifold partremovable from the face mount part, the secondary supply conduitconnected to the manifold part.

FIG. 5 shows the patient interface of FIG. 4 with the manifold partremoved from the face mount part.

FIG. 6 shows a perspective view from the front and to one side of thepreferred form of the face mount part of the preferred form of nasalcannula, the face mount part including a section adapted to receive themanifold part, and a pair of nasal prongs extending from the face mountpart.

FIG. 7 shows a perspective view from the rear and to one side of thepreferred form of the face mount part of the nasal cannula, the facemount part having a pair of nasal prongs extending from the face mountpart, each of the nasal prongs having a gases exit cut-out on their rearface, at the upper part of the prong.

FIG. 8 shows a view directly from the rear of the manifold part of FIG.6, with the gases exit cut-out clearly shown.

FIG. 9 shows a top view of the preferred form of face mount part of thepreferred form of nasal cannula, the view showing the preferred inwardsangle of the nasal prongs relative to a vertical plane which bisects theface mount part, and the preferred alignment of a surface which definesthe perimeter of the cut-out section in the preferred form.

FIG. 10 shows a rear perspective view of the nasal cannula of thepreferred embodiment, the view showing the preferred form and placementof the surface.

FIG. 11 shows a view from under the nasal cannula of the preferredembodiment

FIG. 12 shows an alternate embodiment of the nasal cannula, the cannulaincludes a manifold with two carrier tubes extending from the manifoldand looping around the user's ears and a prong connected to the end ofeach carrier tube.

FIG. 13 shows a further alternative embodiment of the nasal cannulawhere the carrier tubes extend from the manifold, the carrier tubesconnect to the face mount part and the prongs extending from the facemount part

FIG. 14 shows a cross section view of the prongs and manifold, themanifold being engaged with the prongs, the figure also showing thetransition sections and points to measure the rise and run of thetransition sections.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

A preferred form of nasal cannula arrangement is described below withreference to use as part of a patient interface for use in a medicalgases system. It should be noted that the nasal cannula arrangement canbe used with any suitable system that provides a gases stream from agases source to a patient in use. For example, it could be used as partof a system to provide supplementary oxygen to a user, with the oxygenprovided from a source such as a gas bottle or wall outlet. However, itis most suited for a system that provides a heated, humidified, gasesstream to a patient or user. The nasal cannula is suitable for use inthe home or in a hospital environment. The nasal cannula can be variedin size (with the proportions kept generally the same) for use withusers of different sizes. For example, two (or more different sizescould be produced for adult and infant users, but still fall within thescope of the present invention.

First Embodiment

Referring to FIG. 1 a respiratory humidification system such as might beused with a first preferred embodiment of nasal cannula arrangement isshown. A patient or user 1 is receiving a humidified stream of gasesthrough a patient interface 20 which includes the nasal cannulaarrangement and which will be described in detail below. The patientinterface 20 is connected to a delivery conduit 3, the delivery conduit3 being connected between a humidifier unit 2 and the patient interface20. The humidifier unit 2 consists of a humidification chamber 5 that inuse contains a volume of water 6, and a base unit 8. The preferredembodiment of humidification chamber 5 is formed from a plasticsmaterial and in the preferred embodiment includes a conductive base (forexample aluminium) which is in direct contact with a heater plate 7 ofthe humidifier base unit 8. The humidifier base unit 8 is in thepreferred embodiment provided with a control mechanism or electroniccontroller 9 which comprises a microprocessor based controller executingcomputer software commands stored in the controller's memory.

In the preferred form as shown in FIG. 1, the humidifier 2 receivesgases from a gas source unit 15, the gases becoming heated andhumidified as they pass through the chamber 5. It should be noted thatas outlined above, the gas source unit 15 could be replaced orsupplemented by a wall port or a gas bottle. The gas source unit couldbe a gas bottle, a gas blender, a venturi device or a standard blowerunit, or any other suitable system or device that supplies a gasesstream. Humidified gases flow from the humidifier 2 through the deliveryconduit 3 to the patient by way of the patient interface 20.

It should be noted that the system used with the nasal cannula does notrequire the use of a humidifier—that is, the gases stream could be dryand unheated if required. Various types of therapy can be delivered byusing the nasal cannula. The preferred form of therapy will be describedlater. Generally breathing gases and the respiratory gases deliverysystem can be used with the nasal cannula. The respiratoryhumidification described here is just an example of the type of therapyand system the nasal cannula can be used with or as part of.

The controller 9 receives inputs from sources such as user input viadial 10, through which a user of the device may, for example, set apredetermined required value of humidity or temperature of gasessupplied to the patient 1. In response to the user input or input fromany other possible inputs like sensors (for example temperature orhumidity sensors, not shown), the controller 9 determines when, and whatlevel, to energise the heater plate 7 to heat the water 6 within thehumidification chamber 5. As the volume of the water 6 within thehumidification chamber 5 is heated, water vapour begins to fill theremaining volume of the humidification chamber 5. The gases which areprovided to the humidifier unit 2 from the blower unit 15 enter thehumidification chamber 5 above the surface of the water 6, and arehumidified by the water vapour within the humidification chamber as theypass through the chamber 5. The heated humidified gases exit thehumidification chamber 5 through an outlet 4 and are transferred to thepatient interface 20 by the delivery conduit 3.

The preferred form of blower 15 is provided with a variable speed pumpor fan 12 which draws air or other gases through a blower inlet 17. Thespeed of the pump or fan 12 is in the preferred embodiment controlled bya further control apparatus 18. Alternatively control of the pump or fanspeed can be carried out by controller 9. The fan controller 18 can alsobe adapted to receive inputs from sensors in the system, or a user inputfrom a control panel or control unit 19. As noted above, the blower unit15 can be supplemented by or replaced by a gases source such as a gasesbottle or a wall-mounted outlet connected to a central gases source.

The preferred form of delivery conduit 3 includes a heating element 11to prevent condensation of humidified gases occurring within the conduit3 (‘rain out’).

The preferred form of humidification system has been described above,with the nasal cannula described as being included as part of thepatient interface 20. The nasal cannula will now be described in moredetail with particular reference to FIGS. 2 to 5.

Patient Interface

FIG. 2 shows the first embodiment of the patient interface 20 of FIG. 1in more detail. The patient interface 20 broadly consists of a headsecurement mechanism and a nasal cannula arrangement 30, and alsoincludes a gases inlet conduit or secondary supply conduit 62. The headsecurement mechanism enables a user to place and maintain the nasalcannula arrangement 30 in the correct operational position. The gasesinlet conduit or secondary supply conduit 62 forms a fluid or gasesconnection between the outlet end of the main delivery conduit 3 and thenasal cannula arrangement 30 to allow fluids or gases to flow betweenthe main delivery conduit and nasal cannula arrangement. The secondarysupply conduit 62 and detail of the main portion of the nasal cannulaarrangement 30 will be described in detail below.

Head Securement

The preferred and alternative forms of head securement mechanism, whichform part of the patient interface 20, will be described with particularreference to FIGS. 2 and 3. FIG. 2 shows the preferred form of the headsecurement mechanism, while FIG. 3 shows an alternate embodiment of thehead securement mechanism.

In the preferred embodiment, the patient interface 20 is secured to thepatient's head or face by a front strap 50 and rear and top straps 53 aand 53 b, as shown in FIG. 2. The front strap 50 in use connects withthe nasal cannula arrangement 30 and the rear strap 53 a and the topstrap 53 b connect with the front strap 50, the rear strap 53 a wrappingaround the top and back of the patient's head in use. The most preferredform of head strap device is adjustable to allow patients of differentsizes and head shapes to use the nasal cannula arrangement 30. Forexample, an adjustment buckle 54 could be included which allows apatient to loosen or tighten the head strap 53.

Alternatively the patient interface is secured to the patient's head andface by a front strap 50 and a single rear strap 53 a attached to thefront strap 50. The rear strap may be attached to the front strap 50 viaa buckle 54 or alternatively the rear strap 53 a may be integral withthe front strap 50. The buckle 54 allows a patient to loosen or tightenthe side straps in order to achieve a comfortable fit. Alternatively theintegral front and rear straps are elastic and can be stretched over apatients head. The elasticity of the straps exerts a force upon the headto hold the nasal interface in the optimal position when in use. Elasticside straps 50, 53 a can be used with the adjustment buckle 54 or theelastic side straps 50, 53 a may be used on their own without the buckle54.

The head strap arrangement may also include a loop 55 which holds andsupports the secondary supply conduit 62 at or close to the inlet end(described in detail below).

A neck tie or lanyard 63 may also be provided with the patient interface20. FIG. 2 shows an example of a neck tie or lanyard 63. In thepreferred embodiment the neck tie or lanyard 63 is connected to thegases inlet conduit 62 or at a location at or close to the connectionbetween the delivery conduit 3 and the gases delivery conduit 62,supporting the weight of the delivery conduit 3 and the gases inletconduit 62 in use. A toggle 64 is provided with the neck tie 63 to allowadjustment of the neck tie's length. The toggle 64 makes the neck tie 63suitable for any sized patient to use the patient interface 20. The necktie 63 supports the weight of delivery conduit 3 in use, such that theweight does not act on the user or the nasal cannula arrangement 30. Theuse of the neck tie 63 prevents the combined weight of the deliveryconduit 3 and the gases inlet conduit 62 from pulling on the nasalcannula arrangement 30, helping to prevent the nasal prongs 33, 34 frominterfering with the sensitive lining of the nasal passages, or becomingdisplaced or disoriented in use. The preferred embodiment of neck tie orlanyard 63 is loose fitting around the neck so as to preventstrangulation of the user. The lanyard 63 also provides a convenient wayof supporting the delivery conduit 3 and the gases inlet conduit 62.This allows the patient to turn in bed without tugging or pulling on theconduit 3 and helps avoid having the gases inlet conduit 62 fromoverheating under the blankets. In the most preferred form the neck tieor lanyard 63 has a clip that allows the lanyard to be opened and closedby a user in order place and secure the neck tie 63 around a user'sneck. The dip comprises a male and female connector that snap fittogether. The clip is removed by pulling one end of the neck tie 63. Theclip is easily removable and “breaks away” undoing the clip when theuser pulls on one side of the neck tie. This allows the neck tie 63 tobe removed quickly in an emergency situation.

An alternate embodiment of the head securement mechanism is shown inFIG. 3. The nasal cannula arrangement 30 is secured to a patients headwith the aid of over the ear loops 66. The loops 66 are configured tohang over a patient's ears to support the weight of the cannulaarrangement 30. The loops are attached to the nasal cannula arrangementby the side straps 31 (described below) of the nasal cannulaarrangement. The ear loops are horizontally slideable relative to thestraps 31. The horizontal movement capability allows a user to adjustthe tightness of the ear loops to ensure the nasal cannula arrangementfits comfortably and correctly upon a user's face. The loops 66 bear theweight of the nasal cannula arrangement 30, such that the user's nasalpassages are not put under undue stress because of the weight of thenasal cannula arrangement 30. The loops make the cannula arrangement 30more comfortable to wear.

Gases Inlet Conduit

The secondary supply conduit 62 will now be described in detail. Thesecondary supply conduit 62 is a short length of conduit or tubing whichruns between the outlet of the main delivery conduit 3 and the nasalcannula arrangement 30. In use, gases exit the main delivery conduit 3and enter the secondary supply conduit 62, travelling along thesecondary supply conduit 62 to the patient. One reason that secondaryconduits such as the secondary supply conduit 62 are used is as follows:the main delivery conduit 3 is relatively heavy and cumbersome as it isused to transport gases over a reasonably long distance (from thehumidifier unit 2 to a point close to the patient). The main deliveryconduit 3 is therefore required to have a wall that is strong enough tosupport its own weight without collapsing. As the main delivery conduit3 is therefore relatively long (e.g. 8 to 10 feet), this additionallength and the thicker wall structure adds to the weight of the maindelivery conduit 3. If the outlet of the main delivery conduit 3 isconnected directly to the patient interface in such a manner that theuser 2 is required to support this weight, this can cause discomfort tothe user due to the weight of main delivery conduit acting on the user.A lighter, shorter secondary conduit (e.g. secondary supply conduit 62)running between the outlet of the main delivery conduit 3 and thepatient interface 20 is used. Secondary supply conduit 62 is lighter andshorter than the main delivery conduit 3, and as outlined above, isgenerally used with e.g. a neck tie or lanyard 63 connected to thesecondary supply conduit 62 or to the connection between the maindelivery conduit 3 and the secondary supply conduit 62, to support theweight of the main delivery conduit 3 and the secondary supply conduit62 in use.

The connection between the outlet of the main delivery conduit 3 and theinlet of the secondary supply conduit 63 is placed near to the patientto reduce torsion or pulling on the nasal cannula arrangement 30 andreduce possible heat problems or over heating close to the patient dueto the heating element 11 provided in the main delivery conduit 3. Inorder to reduce condensate forming in the unheated secondary supplyconduit 62, a conduit that has vapour transmission properties can beprovided. The secondary supply conduit 62 can be integrally formed withthe main delivery conduit 3 or may be attached by some connectionmechanism, allowing for detachment of the secondary supply conduit 62from the main delivery conduit 3. The connection mechanism can be athreaded screw type connector or a friction locking mechanism. Thesecondary supply conduit may be preferably made from a breathablematerial that allows water vapour to pass through the supply conduit andinto ambient air while substantially preventing liquid water orbreathing gases to pass out of the supply conduit. The supply conduitmay have regions of breathable material along its length oralternatively the entire conduit wall may be breathable. Materials maybe breathable due to their composition, physical structure or acombination thereof. The mechanisms of water vapour transmission throughthese breathable materials are numerous and known in the art. Thepurpose of the breathable region or regions of the supply conduit wallis to allow passage of water vapour from the gases path alongindependent of specific drain locations. This reduces the build up ofcondensation within the breathing tube by drying the humidifiedbreathing gases (by transmitting water vapour to the surrounding ambientair) during their flow through the breathing tube. An example of such amaterial is SYMPATEX™ or GORETEX™ or NAFION™ and so on.

The result of providing a short secondary supply conduit 62 is that amajority of humidity in the gases is transported to the patient, andthere is an insignificant and negligible loss of humidity through thebreathable wall of the short secondary supply conduit, while condensateforming is reduced.

The nasal cannula and its various features will now be described in moredetail.

Nasal Cannula

The preferred form of the nasal cannula 30 which forms part of thepatient interface 20 shall now be described in more detail withparticular reference to FIGS. 4, 5, 6, 7, 8, 9 and 10.

The nasal cannula 30 of the preferred form comprises two main parts: amanifold portion 35 and a face mount part 32. The preferred embodimentsof these two parts will now be described with particular reference toFIGS. 4 and 5.

Manifold Portion

In the preferred form, the manifold portion 35 is in use connected toand in fluid communication with the secondary supply conduit 62 as hasbeen described above. However, it could be connected directly to themain delivery conduit 3 in alternative embodiments. Where the phrase‘gases inlet manifold part’ is used in this specification, this shouldbe taken to mean the manifold portion 35 in combination with thesecondary supply conduit 62, or just the manifold portion 35, asappropriate.

It should also be noted that the preferred form as shown in FIGS. 4 and5 shows the manifold part 35 as being detachable from the remainder ofthe nasal cannula 30. However, the manifold part 35 could also be formedas an integral part of the nasal cannula 30 if preferred orrequired—that is, so that the manifold part 35 and the face mount part32 (described below) are one item.

The preferred form of manifold part 35 is generally tubular in shapehaving a substantially circular inlet 59 on one side that curves to anelongated oval outlet 37, the outlet 37 being formed on one side of themanifold part 35 so that it is perpendicular to the inlet 59. Thecircular inlet 59 in the preferred form receives the patient end of thesecondary supply conduit 62, such that the gases from the secondarysupply conduit 62 can flow through the manifold part 35 (inlet 59 couldalternatively be oval, or any other suitable shape—it does not have tobe circular). In the preferred embodiment the manifold part 35 isintegrated with the secondary supply conduit 62 (i.e. it is not intendedto be removed and replaced repeatedly in use, although it can be removedif required), but alternatively the manifold part 35 could be removablyattached to the secondary supply conduit 62, The manifold part 35engages with the face mount part 32 so that gases can pass through theoutlet 37 and transfer from the secondary supply conduit 62 to thepatient 2 through the nasal prongs 33, 34 (described in detail below).

In the preferred embodiment the manifold part 35 is manufactured from ahard plastic material that only deforms under relatively high loadingconditions (that is, it cannot easily be crushed in the hand of a user).The manifold part 35 may be moulded, injection moulded, machined orcast.

The manifold part 35 in use is connected to the face mount part 32, sothat gases exiting the manifold part 35 enter the face mount part 32.The term “connected” in the context of this specification should betaken to mean either “detachable” or “integral with”, as appropriate.The face mount part will now be described in detail.

Face Mount Part

The face mount part 32 includes the nasal prongs 33, 34, so gasespassing through the face mount part 32 can enter the nasal prongs 33, 34and be delivered to the patient 2. The preferred form of nasal prongs33, 34 extend parallel to each other, curving upwards and inwards fromthe face mount portion 32. In the preferred embodiment, each nasal prongis equidistant from the centre of the face mount part. The structure ofthe prongs 33, 34 will be described in detail below.

The face mount part 32 of the preferred embodiment includes side straps31 and an open tubular recess 38, integrally moulded together as shownin FIGS. 4 and 5. The open tubular recess 38 extends below the facemount part 32 and is adapted to receive the manifold part 35 (for thepreferred embodiment where the face mount part 32 and the manifold part35 are separable items). The face mount part 32 has a lip 39 thatextends around the upper edge of the open tubular recess 38. Themanifold 35 is connected to the face mount part 32 by a friction fit andthe lip 39 on the face mount part 32 helps to grip the manifold part 35and form a strong sealed connection between the manifold part 35 and theface mount part 32. The open tubular recess 38 is divided by a rib 40which extends below the face mount part 32. The rib 40 helps to cradleand hold the manifold part 35 in the correct position as it engages withthe face mount part 32, the rib 38 extending around the outside of themanifold part 35. Outlet 37 on the manifold part 35 aligns in use withthe underside of the face mount 32 portion when the manifold part 35 isconnected to the face mount part 32. This alignment minimises andreduces the amount of gases which leak out of the nasal cannulaarrangement 30, allowing effective treatment of the user by deliveringmaximum amount of humidified gases.

The side straps 31 are used to attach the head strap 50 or the ear loopsto the face mount part 32. The side straps 31 comprise a pair of straps(shown as straps 31 on the figures) which extend from either side of theface mount part 32, and which in the preferred embodiment are formed asan integral part of the face mount part 32. The headgear strap 50 is inuse attached to the side straps 31 so that the patient interface can beworn by a user in use. In the preferred form the ends of the headgearstrap 50 are looped through a pair of slits on the side straps 31, withthe ends including velcro or similar to hold the ends in place when they are looped back on themselves. Alternatively the headgear strap 50 orloops 66 may be clipped onto the side straps 31, for example by way ofco-operating male-female clips, or adhesively attached to the sidestraps 31.

In the preferred embodiment the face mount part, nasal prongs, sidestraps and the open tubular recess are all manufactured as onecontinuous item. The face mount part 32, nasal prongs 33, 34, sidestraps 31 and the open tubular recess 38 are all manufactured out offlexible polymer material or silicone, preferably a soft thermoplasticelastomer (TPE).

The nasal prongs will now be described in more detail.

Nasal Prongs

The following is a description of the nasal prongs. In the followingdescription the term “rear”, or “back” or any such synonym refers tothat part of the structure that faces towards and is closest to thepatients face when the nasal cannula is in use. The term “front” or“forward” or any such synonym refers to the side, face or part whichfaces away from and is furthest away from the face of a user of patientin use. The term “top” or “upper” refers to the side, face or part thatis pointing away from the floor, when a user or patient wearing theinterface is standing or sitting upright and looking forward. The term“bottom” or “lower” refers to the side, face or part that is directed orpointing toward the ground, again when a user or patient wearing theinterface is standing or sitting upright and looking forward.

In the preferred embodiment the face mount part 32 includes two nasalprongs 33, 34 extending upwards and curving inwards from the uppersurface of the face mount part 32 as shown in FIGS. 4, 5, 6 and 7.Referring to FIGS. 7 and 8, the nasal prongs 33, 34 extend from theupper surface of the face mount part 32 and each prong is placed in eachnostril of the patient when the nasal cannula arrangement is in use. Theprongs 33, 34 are configured to deliver gases to a patient. The prongs33, 34 receive humidified gases from the delivery conduit 3 via thesecondary supply conduit 62, the manifold part 35 and the face mountpart 32. It should be noted that in the preferred embodiment, the gasesinlet manifold part 35 receives the gases from the secondary supplyconduit 62, with the gases passing through the gases inlet manifold partto the face mount part 32 and then into the nasal prongs 33, 34. Thenasal prongs 33, 34 are therefore in fluid connection with the gasesinlet manifold part 35 and receive the gases from the secondary supplyconduit 62. As has already been outlined above, the gases inlet manifoldpart 35 and the face mount part 32 could be formed as one item—that is,as a combined manifold and face mount part, and this item could ifrequired be formed to act as a manifold, with the prongs integrallyformed with the manifold, the manifold attaching to one or more gashoses or tubes, in a similar manner to typical nasal cannulae which areknown in the prior art. Where the phrase ‘gases inlet manifold part’ isused in this specification, it should be taken as being broad enough toencompass this arrangement. The phrase should also be taken as beingbroad enough to be inclusive of dual hoses of the type known in theprior art that connect one to each side or end of the manifold tubingand which loop over the ears of a user before attaching to a maindelivery conduit or a secondary supply conduit. It should also be notedthat where the phrase “a gases inlet manifold part adapted to form afluid connection with a delivery conduit” is used, this should be takento mean that the gases inlet manifold part may be directly connected, orindirectly connected with intervening items included such as a secondarysupply conduit, or dual hoses of the type known in the prior art (orboth).

In the preferred embodiment the nasal prongs 33, 34 are generallytubular in shape, with an upwards and rearwards curve. The nasal prongscurve upwards and towards the back of the patient's head when in use.Preferably the prongs are curved toward the back of the patient's nasalpassages, such that the stream of gases delivered by the prongs isdirected toward the back of the patient's nasal passages. The curvatureof the nasal prongs 33, 34 ensures the prongs follow the natural curveof a human's nasal passage. Preferably the prongs follow a curve ofradius 10.5 mm but any radius between 5 and 20 mm is suitable, andlarger or smaller sizes are also possible without departing from thescope of the invention. The curvature of the prongs 33, 34 ensures gasesare delivered into the nasal cavity of the patient and this helps toreduce leakage of gases from the nasal cavity. The curvature of theprongs 33, 34 provides the advantages of added comfort and effectivedelivery of respiratory gases into a patient's nasal cavity.

In the preferred embodiment the nasal prongs 33, 34 fit into thepatient's nasal passage. Preferably each of the nasal prongs aregenerally circular in cross section. Alternatively the nasal prongs maybe triangular or oval in cross section. A circular cross-section is mostadvantageous for use since this shape conforms most closely to the shapeof a human's nasal passage, thus providing a comfortable fit for thepatient and ensuring the correct delivery of the therapy. However, thenostrils and nasal cavities of users are not perfectly circular orgeometrically standard, and other cross-sections (such as the triangularor oval cross sections mentioned above) may be preferable.

In the most preferred form the nasal prongs are arranged equidistantfrom the centre of the face mount part. Preferably the nasal prongs areangled to face slightly inward towards one another as best shown by FIG.9. When viewed from the top, the centre of each of the nasal prongs ispreferably angled 15 degrees inward from the vertical line A as seen onFIG. 9. That is, the angle X between line A and line B, as shown on FIG.9, is 15 degrees. This applies to both of the pair. The line A defines avertical plane, which is substantially parallel to the vertical plane ofsymmetry which bisects the face mount part 32 of the nasal cannula30—that is, a line or plane which would bisect the human nose when thenasal cannula is positioned on the face of a user. The prongs 33, 34 areangled inward towards one another at 15 degrees to provide the mostcomfortable fit when in use. It has been found that having the nasalprongs angled inwards at 15 degrees provides the most comfortable fit orposition for a user and an optimal position for delivering therapeuticgases to a patient. The nasal prongs may be placed at any other anglelarger or smaller than 15 degrees. The range of angles between line Aand line B could for example be between 0 degrees to 60 degrees ofinward angle. Alternatively the nasal prongs could be angled outwardfrom the vertical line A. Angling the nasal prongs outward is notpreferred because angling the prongs outwards means the prongs may notfollow the natural shape of the nasal passage potentially making theprongs uncomfortable to use for most users. However, this may besuitable in some situations, or for some users in certain circumstances.

Each of the nasal prongs includes a gases exit cut-out section 41 on therear side 43 of the nasal prong, as shown in FIGS. 7 and 8 and 10. Thegases exit cut-out or cut-out section in the preferred embodiment giveseach of the prongs the appearance of a scoop. The front side 42 of thenasal prong (the side further away from the patient) extends furtherupwards and inwards from the face mount part 32, and forms a guide wallthat guides humidified gases into the patient's nasal passage when thenasal prongs 33, 34 are in use. The gases exit cut-out in the prong hasa sectional area greater than the cross-sectional area of the prong ator close to the point of entry of gases into the prong from the manifoldsection—that is, the cross-sectional area of the prong is greater at thepoint where the gases exit the prong (and enter the users nare), incomparison to a point at or close to where the gases enter the prongfrom the manifold section.

The cut-out section 41 can be formed in various shapes. In the preferredembodiment the cut-out section 41 is oval in shape when viewed from therear, as best seen in FIG. 8. That is, when viewed from the rear, theperimeter of the cut-out section 41 describes an oval shape, the top ofthe oval angled slightly inwards towards the other nasal prong. Thecut-out section could also be triangular (with one point of the triangleoriented towards the base of the prong, and the other two corners at thetopmost inner edges of the cut-out section 41). The cut-out could alsobe rectangular in shape.

The cut-out can extend from various positions along the nasal prong.Preferably the cut-out section 41 extends from between halfway and twothirds of the Way along the nasal prong, when measured from the top tipof the nasal prong. Alternatively the cut-out section 41 may extend fromless than halfway along the nasal prong, when measured from the top tipof the nasal prong. As a further alternative the cut-out may extend theentire length of the prong. In the most preferred embodiment, thecut-out section 41 extends from between halfway and two-thirds of theway along the nasal prong to provide the best advantages. It has beenfound that having the cut-out extending between halfway and two thirdsensures the optimal size of the opening. Placing the cut-out at thisposition ensures the most optimal size of cut-out to provide theadvantages described later in this specification. For nasal prongsaccording to the preferred embodiment, this corresponds to a cut-outhaving a height of 3 mm to 15 mm. However, the size of the cut-out couldfall outside this range if required for alternative forms.

In the preferred embodiment the cut out 41 is formed during the mouldingprocess. It is preferred that the prongs are moulded by injectionmoulding, casting or vacuum forming. The mould used to produce thedesired prong shape has the cut-out feature built into it.

In alternative embodiments the cut-out section 41 is created by cuttingacross the rear 43 of each of the prongs 33, 34 after these have beenformed in an initial forming operation—e.g. after the face mount part 32has been moulded in an initial forming operation, the cut-out is formedby removing material either by machining or by hand.

The reverse S-shaped surface 80 which defines the cut-out section isbest shown in FIG. 10. The bottom edge of the surface 80 is shown inFIG. 9 as line 800. As can be seen, for each prong, line 800 isperpendicular to a line through the centre of the nasal prong, and isaligned with the rear edge of the prong. This is best shown in FIG. 9.Preferably the surface 80 is shaped as a reverse S shape as shown inFIG. 10. The surface 80 extends a certain distance inward to form thepreferred ‘scoop’ shape of the gases exit cut-out. The reverse S shapeis aligned substantially vertically. The reverse S shaped surfaceproduces the most preferred size and shaped cut-out. After forming, theedges or perimeter of the cut-out section 41 conforms to the surface ofthe reverse S-shaped surface, as shown in FIG. 10. Such a surfaceresults in the optimal cut-out shape that provides the advantagesdescribed below.

In the preferred embodiment the rear wall 43 of the nasal prongs 33, 34also includes a reinforcing feature (not shown in the figures) thatextends upward along the length of the rear wall of the nasal prong. Thereinforcing feature helps to maintains the rear wall 43 of the nasalprong in an upright position. Preferably the reinforcing feature isformed as a ridge running at least part of the way along the rear face43 of the nasal prongs 33, 34. This ridge can he on either the inside orthe outside of the rear wall 43, as the rear wall does not in usegenerally contact the upper lip or nares of a user, and the reinforcingfeature will therefore tend not to interfere with the face of the userand make than uncomfortable. Preferred and alternative forms ofreinforcing feature will be described in greater detail below.

Due to the curvature and shape of the nasal prongs 33, 34, the stream ofair will tend to flow along the front wall of the prongs 33, 34, ratherthan the rear wall 43—the air stream flows along the outside of the bendrather than the inside.

Advantages

The cut-out sections within each nasal prong provide a number ofadvantages. The main advantages are as follows: 1) Each of the prongscan deform or misshape more easily, as they have less structuralrigidity (a piece of their support structure is missing, so they candeform more easily), and are therefore more comfortable in a patient'snasal passage, 2) The gases do not exit from the prong as a jet, througha small aperture. The cut-out provides a larger area of exit aperture atthe exit of the prongs, so that the velocity or air speed of the gasesis reduced at the point where they exit the prong(s). That is, the sizeof the exit aperture (defined by the edge or perimeter of the cut-outsection) is greater than the size or cross-sectional area of the inletaperture, which is defined by the base of the prong where it isconnected to the face mount part 32. The air speed of the gases reducesas the area increases. That is, each prong is shaped so that thevelocity of gases exiting said prong is reduced in comparison to thevelocity of gases at or close to the gases point of entry to the prong.This allows a proportionally greater volume of gases to be delivered toa patient without causing discomfort (in comparison to a cannula prongwhich does not include a cut-out). With the cut-out cannula, air jettingeffects are reduced. The jetting of the airflow is reduced based on thecontinuity equation for energy or mass conservation, which states thatincreasing the cross sectional area equates to a reduction in thevelocity of the airflow. A jet of gas delivered into a user's nasalpassage can irritate or potentially damage the tissue within the nasalpassage. A reduction in the velocity of the flow of gases as deliveredby the nasal prongs reduces irritation in the user's nostrils and thusthe jetting effects. It also follows from the continuity equation thatthe larger the aperture a gas is flowing through, the larger the amountof diffusion. 3) The stream of gases is directed in a generallyrearwards direction (relative to the head of a user) relative to thenasal passage of a user.

These advantages are discussed in more detail below.

The nasal cannula arrangement 30 as shown in FIGS. 6 and 7 is suitablefor the delivery of high airflow, high humidity gas flow to thepatient's nasal cavity. In the preferred embodiment, the cut-out extendsbetween from the top of the prong to between half and two thirds of thedistance to provide the largest cut-out. Further, the shape of thecut-out (reverse S-shape surface as described above) contributes toensuring maximum diffusion and reduction of air jetting effects.

In prior art cannulas, the cannula prongs will generally have an exitaperture which is substantially the same size as their inlet aperture(e.g. where the base of the prong is connected to a manifold). In thecannula of the present invention described above, the size and shape ofthe cut-out helps to reduce the air speed at the point of exit from theprong, and to direct the gases in a generally rearwards direction. Ithas been found that this helps to increase user comfort and compliancewith a therapy regime to a surprising degree. Furthermore, the decreasedvelocity flow of respiratory gases from the cut-out 41 of the nasalprongs 33, 34 helps to ensure that the user will breathe as normally aspossible.

The reduction in air velocity due to the cut-outs in the prongs 33, 34allows the use of a higher flow rate than is generally the case in theprior art. In therapy, high flow rates are preferred in order to meetthe patients requirements. Using high flow rate ensures that wherepossible, the entire volume of an inhaled breath comprises respiratorygases. However, due to increased patient discomfort and potentiallydangerous side-effects with higher flow rates, a trade-off is normallymade between patient comfort/safety, and flow rate. Lower flow ratesthan may be optimal are used to ensure the patient is comfortable enoughto conform with a therapy regime. Using these lower flow rate means atleast part of, and generally a majority of, the user's breath iscomposed of ambient air which can be detrimental to the therapy providedby medical gases. Using relatively higher flow rates and having nasalprongs that allow humidified medical gases to be delivered at high flowrates is advantageous. This helps to ensure that the most efficient andeffective therapy provided to a patient. Surprisingly, it has been foundthat by using the prongs as described above—i.e. prongs that include acut-out section—flow rates between (but not limited to) just above 0L/min to 80 L./min can be delivered to a user and initial user feedbacksuggests that there is decreased discomfort and a greater tendencytowards regime compliance. The prongs can be re-sized—e.g. for use inneonatal applications—without departing from the scope of the invention,with the flow rates or flow range being considerably lower in neonatalapplications. It is anticipated that flow rates of up to 120 L/min couldbe used in certain circumstances. However, it is anticipated that thepreferred range will be in the order of 20-50 L/min for adults, 5-30L/min for Paediatric patients, and just over 0 L/min to 8 L/min forNeonatal patients. The cut-out design is effective at low flow rateswhen used on neonatal patients (as small as 400 gms), where flow ratesof 1-8 L/min would otherwise create very high velocities due to thesmall size of the cannula and patient.

The cut-out sections 41 in the nasal prongs 33, 34 causes the nasalprongs 33, 34 to be more deformable than prior art nasal prongs which donot include cut-outs. Surprisingly, it has been found that the additionof cut-outs does not significantly negatively impact on the gasesdelivery efficiency, and as well as the advantages outlined above,allows the nasal prongs 33, 34 to be bent and flexed to a greater extentthan prior art cannula prongs, to fit comfortably into a patient's nasalpassage. A range of sizes of cannulae will normally be used, to ensure afitment range for all users. However, within each ‘bracket’ or range,the greater bending or flexibility helps improve user comfort. Thecut-out 41 causes the nasal prongs 33, 34 to be more flexible thancompletely “tubular” or round shaped nasal prongs. Generally in use thenasal prongs rest against the nasal mucosa. In other nasal cannulaarrangements the nasal prongs exert a force on the nasal mucosa and thispressure can irritate the user, making wearing nasal prongsuncomfortable. This may even result in damage to the delicate nasaltissue. The gases exit cut-outs 41 within the nasal prongs allow theprongs 33, 34 a greater degree of flexibility within the nasal passage,as the prong pushes against the nasal mucosa tissue. The flexing of theprongs reduces the pressure exerted on the nasal mucosa making it morecomfortable and potentially safer for the user to wear.

The cut out sections 41 within the cannula are also advantageous becausethey have made manufacturing of the cannulas quicker. The cut outsections 41 allow the cannula to be easily lifted off the forming toolby a robot or human operator. The cut-out sections 41 have halved thecycle time.

Reinforcing Feature

Preferably the nasal prongs each include a reinforcing feature 100running along the inner surface of the front wall of the nasal pronghelps the nasal prong to return to its original shape after bending andflexing. This is shown in FIG. 8. Preferably the feature providesstrengthening for the nasal prong against a compressive or tensile forceor both acting on the nasal prong. The feature effectively forms areinforcing spine along the inside surface of the front wall 42 of theprong, with the feature extending upward from the base of the prong andfollowing the contour of the prong. The reinforcing feature 100 acts toallow lateral and rotational movement of the prong and allows the nasalprong to elastically deform in compressive and tensile force directionsand exerts a restorative force to ensure the prong returns to itsoriginal shape. In one embodiment, the reinforcing feature 100 is anupward extending bead running from the base of the prong to the top ofthe prong. In the most preferred form the rib is located along the innersurface of the front wall 42. The bead extends upward from the base ofthe prong to the top of the prong. Preferably the bead extends theentire length of the prong and follows the contour of the prong.Alternatively the bead may only extend a partial height of the prong.Alternatively the bead may be located on the outer surface of the frontwall. In a further alternative form the bead may be located along theback wall, either on the inner or outer surface of the back wall. Thebead is preferably over moulded onto the prong. The reinforcing feature(in this form the bead) is preferably formed from a more rigid materialthan the prongs. The bead is applied to the prong by a co-injectionprocess. The co-injection process involves injection moulding the prongfrom one material, transferring the prong and/or manifold and face mountpart to another tool where the bead material is injection moulded overthe prng The bead acts like a spine to support the prong.

In another form the reinforcing feature 100 may be a rib that extendsupward from the base of the prong, along the height of the prong andfollows the contour of the prong. The rib is preferably located on theinside surface of the front wall 42 but may be located on the outersurface of the front wall 42. Alternatively the rib may be located onthe back wall 43. The rib may be located either on the inner surface orouter surface of the back wall 43. The prong preferably includes aplurality of ribs formed along the inner surface of the front wall. Theribs preferably extend the entire distance of the prong, but mayalternatively only extend a partial distance. The ribs are preferablyidentical to each other in dimensions. The ribs are preferably equallyspaced apart along the prong. The ribs form a skeletal structure thatsupports the prong and reduces deformation of the prongs. The ribs arepreferably formed from a co-injection moulding process as described forthe bead. The ribs are preferably made of a material that is more rigidthan the material used to make the prongs.

The prong may also include a series of ribs (not shown) runninggenerally horizontally across the prong. The ribs maybe used incombination with the reinforcing feature (e.g. the bead) to strengthenthe nasal prongs in compressive and tensile directions, while allowinglateral and rotational movement. Preferably the reinforcing feature,(with or without ribs) is present on the front wall 42 of nasal prong.This is advantageous since this provides the greatest strengthening andalso because the material used for the prongs responds best incompression. Preferably the reinforcing feature is formed integrallywith the nasal prongs during the forming process. Alternatively, areinforcing feature can be attached to the nasal prongs afterforming—e.g. by gluing or ultrasonic welding. Preferably the feature ismade from the same material as the nasal prong. Alternatively thefeature or the ribs could be made from a stiff material such as anotherpolymer material.

The reinforcing feature could alternatively be created by having thefront wall 42 thicker than the backwall 43, when viewed from above. Theincreased thickness of the front wall 42 effectively provides lateraland rotational movement of the prong while providing improved strengthcharacteristics under compressive and tensile loads. The thicker frontwall 42 ensures that the nasal prongs 33, 34 do not collapse or tearwhen subjected to compressive or tensile forces.

A potential problem with “tubular” or “round” nasal prongs of the priorart type is the possibility of creating a seal in the patient's nasalpassage. Although a seal is desirable in certain circumstances if usinge.g. nasal pillows of the type described in WO 2008/014543, in othercircumstances, a seal within the patient's respiratory system can leadto an overpressure being created within the patient's nares. Thisoverpressure can lead to barrotrauma resulting in severe injury andpossible patient death. It can also interfere with the patients naturalbreathing or self-breathing. The additional flexibility and greateraperture size provided to the nasal prongs 33, 34 by the cut-outs 41aids in minimizing the risk of the cannula creating a seal in thepatient's nares. However, it should be noted that a seal is sometimesdesirable, and although in the preferred embodiment, a nasal cannulaarrangement which is not intended to seal has been described, the nasalprongs 33, 34, or the face mount part 32, or both, could be adapted toseal against the nostrils of a user. However, this is not the preferredform.

The flexibility of the side straps 31 allows for easy securement of thenasal cannula arrangement 30 on the user's face since the straps caneasily be bent and flexed to fit around a user's face. The flexibilityof the open tubular recess 38 in the preferred embodiment enables theopen tubular recess 38 to fit around the manifold part 35 and create asecure friction fit or snap on fit. The face mount 32 part is moulded asa single piece of flexible plastic, silicone or rubber material forreliability and ease of use.

The nasal cannula arrangement and the nasal prongs in particular, asshown in FIGS. 2 to 10 are predominantly useful for delivering gaseswith high humidity and high flow rate which is advantageous to thepatient.

Second Embodiment

A second embodiment the patient interface can also be used as part ofthe humidification system as described above in relation to FIG. 1.

The second embodiment of the patient interface broadly consists of ahead securement mechanism substantially similar to that described abovefor the first embodiment, and a nasal cannula arrangement. The headsecurement mechanism is used to attach the patient interface to apatient's face and maintain the position of the patient interface in thecorrect position when in use. The head securement mechanism as describedin relation to FIGS. 2 and 3 can also be used with the second embodimentof the nasal cannula. Alternatively no separate head securementmechanism needs to be used with the nasal interface. This alternativeform of head securement will be described later. The humidificationsystem with which the alternative nasal cannula arrangement is used caninclude a secondary supply conduit 62 similar to that described above,which allows gaseous or fluidic communication between the outlet end ofthe main delivery conduit 3 and the main part of the nasal cannulaarrangement. However, in this alternative form, the secondary supplyconduit 62 and the main delivery conduit 3 can be thought of as a single‘delivery conduit’ in this context.

Nasal Cannula—Second Embodiment

The nasal cannula of the second embodiment will now be described in moredetail. The nasal cannula of the second embodiment comprises 3 mainparts: a pair of carrier tubes, a manifold section, and a pair of nasalprongs, one each of the pair of nasal prongs attached to each of thecarrier tubes, the carrier tubes connected to the manifold section,which is connected to the delivery conduit as outlined above so that astream of gases is delivered to the manifold section. The carrier tubesare used instead of the secondary conduit. The manifold section isformed as a Y-piece connector or a T-piece connector. The carrier tubesare connected to the branches of the Y-piece or T-piece manifoldsection, preferably with a friction fit. Alternatively the carrier tubesmay be connected to the Y- or T-piece by threading or gluing. An evenfurther alternative is the carrier tubes are formed integral to the Y-or T-piece. The Y-piece connector directs flow of gases from thesecondary supply conduit to each of the carrier tubes. Preferably the Y-or T-piece is made of a rigid polymer material, the material rigidenough that it does not readily deform under common operational loads.

The carrier tubes can be attached to a head securement, or they canthemselves be adapted to be used as a head securement mechanism. Thecarrier tubes are wrapped around behind the ears. The carrier tubesallow flexibility for head securement. The carrier tubes are lightenough to wrap around a patient's ears and be comfortable for thepatient to use. The use of carrier tubes makes the entire nasal cannulalight in weight. This can help to increase the comfort level for apatient while using the nasal cannula. The carrier tubes also let peopleof various sizes to use the nasal cannula arrangement as long as thecarrier tubes are long enough to be placed over their ears. The carriertubes connect to the manifold and form a fluid connection with themanifold. The carrier tubes supply breathing gases to the manifold. Themanifold has at least one prong extending from it, the prong deliveringbreathing gases from the manifold to the patient's nasal passage.

In an alternate form a nasal prong is attached to each of the carriertubes at the patient end. The nasal prongs can be detachable from thecarrier tubes. Preferably the nasal prongs are attached to the carriertubes by a friction fit. Alternatively the nasal prongs are threadedinto the carrier tubes. Another alternative is the nasal prongs areglued or attached to the carrier tubes by an industrial adhesive. As afurther alternative the nasal prongs may be integrally formed with thecarrier tubes.

In this alternative form, the prongs are substantially the same asprongs 33, 34 described above for the preferred or first embodiment.Each prong includes a cut-out on the rear side (that part closest to theface of a user in use), which in the preferred form is cut out of therear of each of the prongs so that the edges of the cut-out conform tothe surface of a reverse S-shaped surface.

Features of the Manifold and Prongs

The nasal cannula of the present invention can be used in high flow,high pressure therapy. A stream of gases enters the manifoldsubstantially horizontally because the cannula has a side entrymanifold. The stream of gases flows from the manifold into the prongs,out of the top of the prongs and into a user's nostrils. The inletstream of gases enters the manifold in a substantially horizontaldirection that is approximately orthogonal to the prongs. The inletstream of gases turns through approximately ninety degrees as the gasesflow into and up the prongs such that the stream of gases flowssubstantially aligned with the prongs axis of extension relative to themanifold. In prior art nasal cannula a substantial amount of the gasesgenerally changes direction or turns at the entry of the prongs, whichis a small area at the base of the prongs. The turning of the stream ofgases within the entry to the prong causes the velocity of the gasesstream to reduce. The reduction in flow velocity causes a pressure dropacross the entry of the prongs since the pressure of the gases stream isproportionally related to the velocity of the gases stream. In prior artcannula approximately 65% of the gases stream is turned within the entryof the prongs. The pressure drop is proportional to the radius of theprongs to the power of four. The pressure and velocity drop isundesirable because it reduces the effectiveness of the therapy beingdelivered to the patient. The reduced pressure and velocity may also bedangerous for the patient as the patient may not be getting enoughbreathing gases. In CPAP type treatment the airways of the patient needto be consistently pressurised in order to allow the patient to breatheproperly. A reduction in gases stream pressure due to the pressure dropacross the entry to the prongs can cause the airways of the patient tocollapse due to lack of pressure being supplied to the patient. Thereduction in pressure can also cause the blower speed and power toincrease in order to compensate for the pressure drop. This can bedangerous because the blower may be operating at high speeds. Thepressure and velocity drop can also be adverse to patients receivingventilator therapy because these patients will not receive adequatebreathing pressure and the ventilator can begin to operate outsidenormal operating levels to try and compensate for the pressure andvelocity drop. The prior art cannula may suffer from a pressure drop ofapproximately 25 cm H. sub.2O.

The prongs and manifold of the present invention are shaped and adaptedto turn at least part of the stream of gases inside the manifold ratherthan inside the prongs. FIG. 14 shows details of the prong and manifoldfeatures. The manifold of the present invention is shaped to deflect thestream of gases flowing into the manifold upward in substantially towardthe prong. The manifold includes a manifold chamber defined by the wallsof the manifold. The manifold wall 1400 opposite the upstream prong isangled upward relative the horizontal. The upward angle is labelled.infin. on FIG. 14. Angle .infin. is measured relative to thehorizontal. Angle .infin. is at least 15 degrees upward from thehorizontal. Most preferably angle .infin. is 22 degrees to thehorizontal. Angle .infin. can be angled upward up to 45 degrees. Themanifold includes a scalloped shape 1402 that creates a tooth 1404. Thetooth 1404 allows the manifold 35 to engage with the face mount part 32and the rib 40. The scalloped shape creates a second wall 1403 that issubstantially opposite the downstream prong. The second wall is alsoangled upward from the horizontal at angle a as shown in FIG. 14. Angle.mu. is at least 30 degrees upward from the horizontal. Most preferablyangle .mu. is 33 degrees upward from the horizontal. Angle .mu. can beup to 90 degrees upward from the horizontal.

The prongs 33 and 34 each include transition sections on them. Thetransition sections are contours of the prongs that transition graduallyfrom a substantially horizontal to a substantially upward orientation asshown in FIG. 14. Each prong includes an upstream transition section1500 and a downstream transition section 1501. Each transition section1500, 1501 connecting the horizontally oriented manifold 35 with theupwardly oriented prong 33, 34. The transition sections 1500, 1501 arepreferably curved sections. Alternatively the transition sections 1500,1501 may be straight sections or chamfers that connect the horizontallyoriented manifold with the upwardly oriented prong. Preferably theupstream transition section 1500 has a shallower curve than thedownstream transition section 1501. In the alternate form where thetransition sections 1500, 1501 are straight line section, the downstreamtransition section 1501 is at a steeper angle than the upstreamtransition section 1500. In a further alternative form the transitionsections 1500, 1501 may consist of multiple straight line sections. Thedownstream transition section 1501 comprises of straight line sectionsthat are steeper than the upstream transition section 1500.

The transition sections 1500, 1501 change from a horizontal orientationto a vertical orientation within an area, meaning the section 1500 and1501 transition from a horizontal to a vertical within an area. The areaof transition is defined by vertical rise and a horizontal run. The riseand run are measured from specific points on the prongs. Preferably therun is the horizontal distance between a tangent point to the horizontalmanifold and the narrowest point of the prong. Fox the upstreamtransition section 1500 the tangent point of the horizontal manifold isshown as point A and the narrowest point of the prong is shown as pointB, in FIG. 14. Point B is the narrowest point of the prong because theprong extends in three dimensions. The prong extends upward and towardthe patient. The narrowest point of the prong is point B due to thecurved profile of the prong. Alternatively the horizontal run may be thedistance between the point where the prong begins to transition from thehorizontal and the narrowest point of the prong. In a furtheralternative the horizontal run may be the horizontal distance between apoint tangent to the horizontal manifold (point A) and the point tangentto the prong when the prong is substantially vertical. The point tangentto the prong when the prong is substantially vertical is point E asshown in FIG. 14. The prong being substantially vertical as referred toearlier is in context of FIG. 14 only, relative to the prongs whenviewed from the back of the prongs. In reality the prongs extend upwardand backward, but FIG. 14 shows a cross section view of the prongs andmanifold assembly. Vertical as referred to in the specification, withreference to point D is in context of the prongs as viewed in FIG. 14.The vertical rise is preferably the vertical distance between points Aand B. In an alternate form the vertical rise may be calculated as thevertical distance between points A and E.

For the downstream transition section the horizontal run is alsopreferably measured from a point that is tangential to the horizontalmanifold 35 to the narrowest of the prong. Point D on FIG. 14 is a pointtangent to the horizontal manifold for the downstream transition section1501. Point C is the narrowest point of the prong on the downstreamtransition section 1501. Alternatively the run for the downstreamtransitional section may be measured to the point where the prong issubstantially vertical, point F in FIG. 14. In reality the prong isangled toward the patient and the prong curves. FIG. 14 shows a crosssection and shows the prong as being substantially vertical in crosssection. Point F is the point where the prong becomes substantiallyvertical in cross section. Point F is only referenced with respect toFIG. 14. Preferably the run for the downstream section is the horizontaldistance between point D and point C. Alternatively the horizontal runof the downstream transition section may be the horizontal distancebetween point D and point F, as seen in FIG. 14. The vertical rise ofthe downstream transition section 1501 is the vertical distance betweenpoint D and point C. Alternatively the vertical rise for the downstreamtransition section 1501 may be the vertical distance between point D andpoint F.

In the most preferred form the vertical rise of the upstream transitionsection 1500 and downstream section 1501 is substantially equal to eachother. In the most preferred form the vertical rise of the upstream anddownstream transition sections 1500, 1501 is exactly identical.Preferably the horizontal run of the upstream transition section 1500 isbetween one to two times larger than the horizontal run of saiddownstream transition section 1501. Most preferably the horizontal runof the upstream transition section 1500 is one and a half times largerthan the horizontal run of the downstream transition section 1501.

In the alternative form where the transition sections 1500, 1501 arestraight line sections, the transition sections extend upward from thehorizontal manifold at an angle. The alternate upstream transitionsection 1500 extends upward at angle of a as shown in FIG. 14. Thealternate downstream transition section 1501 extends upward at angle.beta. as shown in FIG. 14. Preferably angle .beta. is larger than angle.alpha. Preferably angle .beta. is between 1.1 and 2.5 times larger thanangle .alpha. In the most preferred form angle .beta. is 1.5 timeslarger than angle .alpha. Preferably angles .beta. and .alpha. arebetween 35 degrees and 65 degrees. In the most preferred form angle.beta. is 33 degrees and angle .alpha. is 22 degrees. The ratios andrelationships between the upstream and downstream transition sectionsdescribed hold true for varying sized cannulae.

The upstream transition section 1500 having a shallower curve than thedownstream transition is advantageous. The shallower curve of theupstream transition section 1500 guides a substantial part of the gasesstream into the prongs. The downstream transition section 1501 being asharper or steeper forces a substantial part of the gases stream to turnwithin the manifold before entering the prongs. The shape of thedownstream transition section 1501 restricts the amount of turning ofthe gases stream within the prong. This allows a substantial part of thegases stream to enter the prong in a direction substantially aligned tothe prongs 33, 34. The gases stream turning in the manifold 35 resultsin a reduced pressure drop and reduced velocity drop of the gases streamas compared to gases stream turning within the prong itself. Theshallower curve or the upstream transition section 1500 and the shape ofthe manifold provide a larger effective diameter of the prong. Thisresults in a lower pressure drop as compared to the gases stream turninginside the prongs. The transition sections 1500, 1501 and the shape ofthe transition sections forces approximately 65% of the gases stream toturn inside the manifold flow chamber. The horizontal run of theupstream transition section 1500 being larger than the run of thedownstream transition section also provides for a larger effectivediameter of the prong. The larger run of the upstream stream transitionsection allows for the gases to turn in the manifold resulting in lesspressure and velocity drop. This is advantageous for the user becausethe correct amount of gases is delivered at the correct pressure andvelocity. This results in more effective therapy being delivered to theuser. While the invention is susceptible to embodiment in differentforms, specific embodiments are shown in the drawings, and described indetail above. The present disclosure is to be considered anexemplification of the principles of the invention, and is not intendedto limit the invention to that as illustrated and described herein.

What is claimed is:
 1. A cannula arrangement comprising: a gases inletmanifold part configured to receive a gases flow; at least one elongateprong in fluid connection with said gases inlet manifold part, said atleast one elongate prong being configured to be inserted into one ormore airways of a patient, the gases flow passing through said gasesinlet manifold part and through said at least one elongate prong; saidat least one elongate prong having a rear side and a front side, whereinsaid rear side is closer to the patient when in use and said front sideis further from the patient when in use; face mount parts extendinglaterally outward from said at least one elongate prong, said face mountparts being adapted to connect to a headgear assembly, said face mountparts being attached to said gases inlet manifold part, said face mountparts being adapted to rest against a portion of a face of the patientto stabilize said cannula arrangement; and said at least one elongateprong has a reinforcing feature to provide structural rigidity to saidat least one elongate prong and to prevent collapse of said at least oneelongate prong in at least one axis, said reinforcement feature furtherconfigured to prevent collapse of said at least one elongate prong inresponse to a tensile force or a compressive force.
 2. A cannulaarrangement as claimed in claim 1, wherein said at least one elongateprong is connected to said gases inlet manifold part by a pair ofcarrier tubes, said pair of carrier tubes being in fluid communicationwith said at least one elongate prong and said gases inlet manifoldpart, and said pair of carrier tubes being configured to transport gasesfrom said gases inlet manifold part to said at least one elongate prong.3. A cannula arrangement as claimed in claim 2, wherein said gases inletmanifold part is a Y piece or a T piece.
 4. A cannula arrangement asclaimed in claim 1, wherein said at least one elongate prong comprises agases exit cut out on said rear side of said at least one elongateprong, said gases exit cut out having a cross sectional area greaterthan a cross sectional area of said at least one elongate prong at orclose to a point of entry of the stream of gases into said at least oneelongate prong, a plurality of edges of said gases exit cut outconforming to a surface that is substantially reverse S shaped.
 5. Acannula arrangement as claimed in claim 4, wherein said substantiallyreverse S shape is aligned vertically, said front side extending furtherupwards and rearwards than said rear side, said front side forming aguide wall that guides the gases flow into the one or more airways ofthe patient when in use.
 6. A cannula arrangement as claimed in claim 4,wherein said gases exit cut-out extends between halfway and two-thirdsof a total length of said at least one elongate prong with said gasesexit cut-out being measured from a tip of said at least one elongateprong.
 7. A cannula arrangement as claimed in claim 4, wherein saidgases exit cut-out has a height of between 3 mm and 15 mm.
 8. A cannulaarrangement as claimed in claim 1, wherein the one or more airways ofthe patient is any of a nasal passage and an oral passage.
 9. A cannulaarrangement as claimed in claim 1, wherein said cannula arrangement is anasal cannula arrangement, said at least one elongate prong being a pairof prongs, each of said pair of prongs being configured to be insertedinto a corresponding nare of the patient.
 10. A cannula arrangement asclaimed in claim 1, wherein said at least one elongate prong is angledbetween 5 and 20 degrees inward relative to a vertical planar line thatbisects said face mount parts.
 11. A cannula arrangement as claimed inclaim 1, wherein said at least one elongate prong is angled 15 degreesinward relative to a vertical planar line that bisects said face mountparts.
 12. A cannula arrangement as claimed in claim 4, wherein a loweredge of said surface cuts across said rear side of said at least oneelongate prong to create said gases exit cut-out.
 13. A cannulaarrangement as claimed in claim 1, wherein said reinforcing feature isformed as a substantially vertical ridge or spine running at least partof a total length of said front side or said rear side of said at leastone elongate prong.
 14. A cannula arrangement as claimed in claim 1,wherein said reinforcing feature is a plurality of ribs formedintegrally with said at least one elongate prong, said plurality of ribsextending laterally across said front side of said at least one elongateprong.
 15. A cannula arrangement as claimed in claim 1, wherein saidreinforcement feature is integrally formed with said at least oneelongate prong.
 16. A cannula arrangement as claimed in claim 1, whereinsaid reinforcement feature comprises a thickened portion, said thickenedportion can be positioned on said front side or said rear side of saidat least one elongate prong.
 17. A cannula arrangement as claimed inclaim 1, wherein said cannula arrangement further comprises side strapsadapted to allow a securement assembly to be connected to said cannulaarrangement so that said cannula arrangement can be secured to thepatient in use.
 18. A system for delivering respiratory gases to apatient, said system comprising: a gas source unit adapted to provide astream of gases; a patient interface; a delivery conduit adapted toreceive the stream of gases from said gas source unit and adapted tocarry the stream of gases from said gas source unit to said patientinterface, said patient interface being a cannula arrangement as claimedin claim
 1. 19. A system for delivering respiratory gases as claimed inclaim 18, wherein said system is adapted to deliver high flow gases in arange of just over 0 L/min to 120 L/min.
 20. A system for deliveringrespiratory gases as claimed in claim 18, wherein said system isconfigured to deliver high flow medical gases such that inhaled gases ofthe patient comprises a majority of gases from the stream of gases and aminimal percentage of ambient air.